Pharmacovigilance Coordinator

Job SummaryAs a Global Pharmacovigilance Coordinator at Medpace, you will be responsible for coordinating pharmacovigilance activities across multiple regions.Key ResponsibilitiesCollaborate with cross-functional teams to ensure compliance with regulatory requirementsDevelop and maintain safety databases and associated documentationCoordinate safety-related...

Job Description: Pharmacovigilance CoordinatorThis Pharmacovigilance Coordinator role is a critical part of our team at Medpace. We're seeking an experienced individual to coordinate the collection, processing, and tracking of serious adverse event reports, generate safety narratives and queries, and perform quality control of safety cases.Key...

Job Overview: Medpace, Inc. is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. As a Global Pharmacovigilance Coordinator, you will play a critical role in accelerating the global development of safe and effective medical...

Are you a skilled professional looking for a challenging role in clinical pharmacovigilance? We are seeking an experienced Clinical Pharmacovigilance Specialist to join our team at Medpace in Stirling, Scotland. As a key member of our Clinical Safety department, you will play a vital role in ensuring the safety of patients participating in clinical...

Job DescriptionIn this role, you will collect, process, and track serious adverse event reports to support the development of life-changing medicines.Main ResponsibilitiesCollect, process, and track SAE reports.Generate safety narratives and queries.Perform quality control of safety cases.Prepare clinical safety documents.Attend internal and external...

About the RoleMedpace is seeking a highly skilled Clinical Safety Coordinator - EMEA to join our European Pharmacovigilance team. This role involves coordinating clinical trial projects, ensuring client deliverables are met, and providing oversight and compliance reports. Additionally, the successful candidate will develop presentation material and present...

Medpace is seeking a skilled Global Adverse Event Coordinator to join our Clinical Safety team in Stirling, Scotland. As a key member of our team, you will play a vital role in ensuring the safe conduct of clinical trials by identifying and managing potential risks associated with investigational products.The estimated salary for this position is £35,000 -...

About the RoleWe are seeking a skilled Clinical Safety Coordinator to join our team. The successful candidate will be responsible for collecting, processing, and tracking SAE reports to support the development of life-changing medicines.Key ResponsibilitiesCollect, process, and track SAE reports.Generate safety narratives and queries.Perform quality control...

About the Role:We are seeking a highly motivated Clinical Safety Specialist to join our European Pharmacovigilance team in Stirling. As a key member of our Clinical Safety group, you will work closely with Medical Monitors, Quality Assurance, and Clinical Trial Management to ensure the timely collection, processing, and tracking of serious adverse event...

Job DescriptionWe are seeking a skilled Clinical Safety Specialist to join our Pharmacovigilance team at Medpace in Stirling. In this role, you will work closely with cross-functional teams to collect, process, and track serious adverse event reports, generate safety narratives and queries, and perform Safety Database data entry, quality control review, and...

About the Role: Medpace, Inc. is seeking a skilled Clinical Safety Specialist to join its European Pharmacovigilance team in Stirling. The successful candidate will be responsible for collecting, processing, and tracking serious adverse event reports.Main Responsibilities:Generate safety narratives and queries.Safety Database data entry.Perform quality...

We are seeking a highly skilled Senior Safety Professional to join our Clinical Safety team at Medpace in Stirling, Scotland. In this role, you will play a critical part in ensuring the safe conduct of clinical trials by identifying and mitigating potential risks associated with investigational products.The estimated salary for this position is £50,000 -...

Job OverviewThis role involves collecting, processing, and tracking serious adverse event reports to support the development of life-changing medicines.ResponsibilitiesCollect, process, and track SAE reports for the development of life-changing medicines.Generate safety narratives and queries to ensure compliance with GCP Guidelines.Perform quality control...

Clinical Safety Specialist Job Summary:We are seeking a skilled Clinical Safety Specialist to join our team in Stirling. As a key member of our Clinical Safety group, you will work closely with Medical Monitors, Quality Assurance, and Clinical Trial Management to ensure the timely collection, processing, and tracking of SAE reports.Key...

Job Summary: **Where you’ll work** Based at either our Stirling or London office, Medpace offers hybrid working solutions upon completion of probation. Company sponsorship in not available for this role. Responsibilities: - Collect, process, and track serious adverse event (SAE) reports - Generate safety narratives and queries - Safety Database data...